A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029048



Internal ID19118267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115009504..115072439hg38UCSC Ensembl
Innerchr5:114345201..114408136hg19UCSC Ensembl
Innerchr5:114373100..114436035hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3862936
hg1962936
hg1862936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647082
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029048
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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